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CS-W001157 4
Total: USD 88.00

(R)-1-(4-Bromophenyl)ethylamine

  • CAS No. 45791-36-4

  • Cat. No. CS-B0174
  • Purity≥96%
  • MDL No.MFCD00066025
  • HazMat Fee +

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    Each bottle is packed as an Excepted Quantity, with a maximum of 1g for items in class 6.1 packing group I or II, and up to 25g for all other hazardous materials.

    If shipping is charged to your FedEx account, the HazMat fee will be billed directly by the courier. Otherwise, the fee will be included on your invoice. To help you avoid the HazMat fee, we can package a 5g order of a class 6.1 packing group I or II material as five separate 1g units, and a 100g order of any other dangerous good as four 25g units. This packaging adjustment will be made unless you instruct otherwise on your purchase order. Below, you will find the fee schedule from FedEx for handling hazardous materials.

    Type
    HazMat Fee
    Excepted Quantity $0.00
    FedEx Limited Quantities Ground $0.00
    Hazmat Ground shipping $50.00+
    Inaccessible (Haz class 6.1 or 9), Domestic $68.00+
    Accessible (Haz class 3, 4, 5 or 8), Domestic $158.00+
    Inaccessible (Haz class 6.1 or 9), International $108.00+
    Accessible (Haz class 3, 4, 5 or 8), International $238.00+

    An item is classified as a dangerous good if our website displays Hazardous Material (HazMat) information for it.

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*For research and further manufacturing use only, not for direct human use.

(R)-1-(4-Bromophenyl)ethylamine|CS-B0174

Structure of 45791-36-4

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Description

(R)-1-(4-Bromophenyl)ethylamine is a chiral building block featuring a pendant bromophenyl group and a stereodefined amine center. This configuration enables selective incorporation into asymmetric syntheses, particularly in pharmaceutical intermediates where enantioselectivity is critical. The molecule exhibits enhanced stability under standard bench conditions and integrates readily into multi-step reaction sequences.

Application

(R)-1-(4-Bromophenyl)ethylamine serves as a chiral building block for asymmetric synthesis, enabling stereoselective construction of biologically relevant scaffolds. Its bench-stable nature and tolerance to common functional groups facilitate straightforward incorporation into medicinal chemistry workflows. The pendant bromide supports further diversification via palladium-catalyzed cross-coupling reactions, making it a versatile intermediate for API development.

General Information

  • CAS No. 45791-36-4
  • Cat. No. CS-B0174
  • Purity ≥96%
  • MDL No. MFCD00066025
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₁₀BrN
  • Molecular Weight 200.08
  • Synonym(s) (R)-(+)-p-Bromo-alpha-methylbenzylamine
  • SMILES N[C@H](C)C1=CC=C(Br)C=C1

Computational Chemistry Data

  • TPSA   26.02
  • LogP   2.4688
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   1

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS05,GHS09
Signal Word : Danger
UN#: 2735
Class : 8
Packing Group : Ⅲ
Hazard Statements : H302-H314-H411
Precautionary Statements : P260-P264-P270-P273-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P330-P363-P391-P405-P501

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